P. Sham

Publication List Details

Period

2001 - 2008

Number

26

Co-Authors

Linkage to chromosome 1p36 for Attention Deficit Hyperactivity Disorder traits in school and home settings (2008)

Zhou, K., Asherson, P., Sham, P., Franke, B., Anney, R.J., Buitelaar, J., ...

Background Limited success has been achieved through previous attention-deficit/hyperactivity disorder (ADHD) linkage scans, which were all designed to map genes underlying the dichotomous phenotype....

DSM-IV combined type ADHD shows familial association with sibling trait scores: A sampling strategy for QTL linkage (2008)

Chen, W., Zhou, K., Sham, P., Franke, B., Kuntsi, J., Campbell, D., ...

Attention deficit hyperactivity disorder (ADHD) is a discrete clinical syndrome characterized by the triad of inattention, hyperactivity, and impulsivity in the context of marked impairments....

The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes (2006)

Brookes, K, Xu, X, Chen, W, Zhou, K, Neale, B, Lowe, N, ...

Attention deficit hyperactivity disorder (ADHD) is a common neurodevelopmental disorder, starting in early childhood and persisting into adulthood in the majority of cases. Family and twin studies...

The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes (2006)

Brookes, K., Xu, X., Chen, W., Zhou, K., Neale, B., Lowe, N., ...

Attention deficit hyperactivity disorder (ADHD) is a common neurodevelopmental disorder, starting in early childhood and persisting into adulthood in the majority of cases. Family and twin studies...

An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder (2005)

Curran, S., Roberts, S., Thomas, S., Veltman, M., Browne, J., Medda, E., ...

Autism (OMIM 209850) is a neurodevelopmental disorder with a significant genetic component of a complex nature. Cytogenetic abnormalities in the Prader-Willi/Angelman syndrome critical region (PWACR)...

Is the P300 wave an endophenotype for schizophrenia? A meta-analysis and a family study (2005)

Bramon, Elvira, Croft, Rodney J., Filbey, F., Frangou, S., Gruzelier, J. H., Landau, S., ...

Introduction: We assessed the usefulness of the P300 wave as endophenotype for schizophrenia by means of a meta-analysis of the literature as well as our own family study. Method: Meta-analysis: We...

Is the P300 wave an endophenotype for schizophrenia? A meta-analysis and a family study (2005)

Bramon, Elvira, Croft, Rodney J., Filbey, F., Frangou, S., Gruzelier, J. H., Landau, S., ...

Introduction: We assessed the usefulness of the P300 wave as endophenotype for schizophrenia by means of a meta-analysis of the literature as well as our own family study. Method: Meta-analysis: We...

Is the P300 wave an endophenotype for schizophrenia? A meta-analysis and a family study (2005)

Bramon, Elvira, Croft, Rodney J., Filbey, F., Frangou, S., Gruzelier, J. H., Landau, S., ...

Introduction: We assessed the usefulness of the P300 wave as endophenotype for schizophrenia by means of a meta-analysis of the literature as well as our own family study. Method: Meta-analysis: We...

Is the P300 wave an endophenotype for schizophrenia? A meta-analysis and a family study (2005)

Bramon, Elvira, Croft, Rodney J., Filbey, F., Frangou, S., Gruzelier, J. H., Landau, S., ...

Introduction: We assessed the usefulness of the P300 wave as endophenotype for schizophrenia by means of a meta-analysis of the literature as well as our own family study. Method: Meta-analysis: We...

Is the P300 wave an endophenotype for schizophrenia? A meta-analysis and a family study (2005)

Bramon, Elvira, Croft, Rodney J., Filbey, F., Frangou, S., Gruzelier, J. H., Landau, S., ...

Introduction: We assessed the usefulness of the P300 wave as endophenotype for schizophrenia by means of a meta-analysis of the literature as well as our own family study. Method: Meta-analysis: We...

An association analysis of microsatellite markers across the Prader Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder (2004)

Curran, S.R., Roberts, S., Thomas, S., Veltman, M., Browne, J., Medda, E., ...

Autism (OMIM 209850) is a neurodevelopmental disorder with a significant genetic component of a complex nature. Cytogenetic abnormalities in the Prader-Willi/Angelman syndrome critical region (PWACR)...

An association analysis of microsatellite markers across the Prader Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder (2004)

Curran, S.R., Roberts, S., Thomas, S., Veltman, M., Browne, J., Medda, E., ...

Autism (OMIM 209850) is a neurodevelopmental disorder with a significant genetic component of a complex nature. Cytogenetic abnormalities in the Prader-Willi/Angelman syndrome critical region (PWACR)...

Attention deficit hyperactivity disorder (ADHD) and the dopamine D4 receptor gene: evidence of association but no linkage in a UK sample (2001)

Mill, J., Curran, S., Kent, L., Richard, S., Gould, A., Virdee, V., ...

Recent studies report association and linkage between attention deficit hyperactivity disorder (ADHD) and the 7-repeat allele of a 48 base-pair repeat in the dopamine D4 receptor gene (DRD4).1 We...

Attention defecit hyperactive disorder (AD/HD) and the dopamine D4 receptor gene: evidence of association but no linkage in a UK sample. (2001)

Mill, J., Curran, S., Kent, L., Richards, S., Gould, A., Virdee, V., ...

Recent studies report association and linkage between attention deficit hyperactivity disorder (ADHD) and the 7-repeat allele of a 48 base-pair repeat in the dopamine D4 receptor gene (DRD4).1 We...

Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mapping.

Ohadi, M, Lalloz, M R, Sham, P, Zhao, J, Dearlove, A M, Shiach, C, ...

Familial hemophagocytic lymphohistiocytosis (FHL), also known as familial erythrophagocytic lymphohistiocytosis and familial histiocytic reticulosis, is a rare autosomal recessive disorder of early...

Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mapping.

Ohadi, M, Lalloz, M R, Sham, P, Zhao, J, Dearlove, A M, Shiach, C, ...

Familial hemophagocytic lymphohistiocytosis (FHL), also known as familial erythrophagocytic lymphohistiocytosis and familial histiocytic reticulosis, is a rare autosomal recessive disorder of early...

Cytochrome P4502D6 genotype does not determine response to clozapine.

Arranz, M J, Dawson, E, Shaikh, S, Sham, P, Sharma, T, Aitchison, K, ...

1. The atypical antipsychotic drug clozapine, used in the treatment of resistant schizophrenia, is metabolized partly by the hepatic cytochrome P450 enzyme CYP2D6. Two phenotypes with respect to the...

Familial psychiatric presentation of Huntington's disease.

Lovestone, S, Hodgson, S, Sham, P, Differ, A M, Levy, R

Symptoms of schizophrenia may be encountered in Huntington's disease (HD) but usually when the full clinical syndrome is apparent; prechoreic psychosis is relatively uncommon. We describe a family...